Product Recalls in Tennessee
Product recalls affecting Tennessee — including food, drugs, consumer products, medical devices, and vehicles distributed to Tennessee. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,580 recalls have been distributed to Tennessee in the last 12 months.
Showing 19481–19500 of 29,188 recalls
Recalled Item: Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems...
The Issue: All lots of modular neck hip prostheses are being recalled due to a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Definition Flash System Recalled by Siemens Medical Solutions USA,...
The Issue: Software update that provides software and firmware bug-fixes to improve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Spectral CT Applications supports viewing and analysis of images...
The Issue: A software defect is causing issues with the IQon Spectral CT and Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT is a Computed Tomography X-Ray System intended Recalled by...
The Issue: A software defect is causing issues with the IQon Spectral CT and Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 728232 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 728231 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 728323 Recalled by Philips Medical Systems (Cleveland)...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.0 Recalled by RAYSEARCH LABORATORIES AB Due to Software...
The Issue: Software anomaly; an issue was found with the proton Pencil Beam Scanning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAM Kirschner Wire Recalled by Stryker Howmedica Osteonics Corp. Due to A...
The Issue: A review of packaging revealed the seal integrity of the pouch may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Regular Set Wash Material Recalled by Ivoclar...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...
The Issue: Drapes within the affected lots may include a manufacturing variation that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Test Pack Heavy/Light Fast Set Recalled by Ivoclar Vivadent, Inc....
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnControl Biopsy System Ported Needle Tray Recalled by Teleflex Medical Due...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Lesion Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.